Symmetry QUAD-LOCK® 50-9006

GUDID 00887482021040

PAPER LABEL W/INDICATOR SMALL

SYMMETRY SURGICAL INC.

Sterilization container filter Sterilization container filter Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use Sterilization container filter, single-use

Primary Device ID	00887482021040
NIH Device Record Key	733ac884-88c6-4c9c-952d-b4942d15eab2
Commercial Distribution Discontinuation	9999-01-01
Commercial Distribution Status	In Commercial Distribution
Brand Name	Symmetry QUAD-LOCK®
Version Model Number	50-9006
Catalog Number	50-9006
Company DUNS	079641356
Company Name	SYMMETRY SURGICAL INC.
Device Count	1
DM Exempt	true
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887482021040 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K120117

FDA Product Code

KCT	Sterilization Wrap Containers, Trays, Cassettes & Other Accessories